FORTITUDE CEMENT RESTRICTOR— 510(k) K021719

Unknown

Spinal Concepts, Inc.

FDA 510(k) clearance K021719 for FORTITUDE CEMENT RESTRICTOR, Unknown on 2002-08-15. Applicant: Spinal Concepts, Inc.. Device class: 2.

Clearance details

Applicant: Spinal Concepts, Inc.
Product code: Code JDK
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2002-05-23
Decision date: 2002-08-15
Decision: Unknown
Clearance type: Traditional
Location: Austin, TX, US

Download summary PDF View on FDA.gov ↗

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K033663 — SPINAL CONCEPTS INC. CODA2004-05-27
K033517 — SPINAL CONCEPTS INC. CADENCE AND TRAXIS2004-02-18

Data sourced from openFDA. This site is unofficial and independent of the FDA.